510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K113051Substantially Equivalent

Spacelabs Arkon Anesthesia Workstation

GE Healthcare, Nederland CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K113051 is the FDA 510(k) clearance record for SPACELABS ARKON ANESTHESIA WORKSTATION, a class II device, cleared for Spacelabs Healthcare on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show 6 recalls naming K113051.

Clearance record

Decision date
Received
(161 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Spacelabs Healthcare P.O. Box 3018, Nederland CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260